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rs4087296

From SNPedia

Orientationplus
Stabilizedplus
Make rs4087296(C;C)
Make rs4087296(C;T)
Make rs4087296(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position82344176
is asnp
is mentioned by
dbSNPrs4087296
ebirs4087296
HLIrs4087296
Exacrs4087296
Varsomers4087296
Maprs4087296
PheGenIrs4087296
hapmaprs4087296
1000 genomesrs4087296
hgdprs4087296
ensemblrs4087296
gopubmedrs4087296
geneviewrs4087296
scholarrs4087296
googlers4087296
pharmgkbrs4087296
gwascentralrs4087296
openSNPrs4087296
23andMers4087296
23andMe allrs4087296
SNP Nexus

SNPshotrs4087296
SNPdbers4087296
MSV3drs4087296
GWAS Ctlgrs4087296
GMAF0.2856
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Bone mineral density
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 2.9999999999999999E-7
Odds Ratio NR NR

[PMID 17903299OA-icon.png] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.

[PMID 19629617OA-icon.png] Replication study of candidate genes/loci associated with osteoporosis based on genome-wide screening.


GET Evidence
rs4087296
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.367188
summary